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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850286Generated: October 30, 2026

Methyl iodide → Methyl 1-methyl-1H-benzimidazole-2-carboxylate

https://huagongshe.com/reaction/1850286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 1H-1,3-benzodiazole-2-carboxylateHCID 576526—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 1-methyl-1H-benzimidazole-2-carboxylateHCID 280259894.6%

Reaction Steps

To a solution of 1H-benzoimidazole-2-carboxylic acid methyl ester (18) (177 mg, 1.0 mmol) in dry DMF (5 mL) was added sodium hydride (applied as 60% dispersion in oil, 62 mg, 1.5 mmol)) at 0° C. under N2 atmosphere. After 0.5 h, iodomethane (284 mg, 2.0 mmol) was added slowly. The reaction mixture was stirred at RT for 4 h. The reaction was diluted with brine at 0° C. and extracted with EtOAc (3×20 mL). The combined organics were washed with water (2×15 mL), brine (20 mL), dried over sodium sulfate and filtered. The filtrate was concentrated and purified by flash column chromatography to provide the title compound (81) (180 mg, 90% yield) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-a02f0e1aa4e3487a86fe7e7839464264
Source noteuspto-grants-2015_02